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rs878855041

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855041(-;-)
Make rs878855041(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position80081603
GeneCCDC40
is asnp
is mentioned by
dbSNPrs878855041
ebirs878855041
HLIrs878855041
Exacrs878855041
Varsomers878855041
Maprs878855041
PheGenIrs878855041
hapmaprs878855041
1000 genomesrs878855041
hgdprs878855041
ensemblrs878855041
gopubmedrs878855041
geneviewrs878855041
scholarrs878855041
googlers878855041
pharmgkbrs878855041
gwascentralrs878855041
openSNPrs878855041
23andMers878855041
23andMe allrs878855041
SNP Nexus

SNPshotrs878855041
SNPdbers878855041
MSV3drs878855041
GWAS Ctlgrs878855041
Max Magnitude0
ClinVar
Risk rs878855041(;)
Alt rs878855041(;)
Reference rs878855041(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene CCDC40
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000017.10:g.78055402delC
CLNSRC
CLNACC RCV000230208.1,